Effect of Mental Imagery in Patients With Persistent Post-concussion Symptoms

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-74
SponsorReuth Rehabilitation Hospital

About this trial

Background: Mild Traumatic Brain Injury (mTBI) often results in persistent emotional, cognitive, and somatic symptoms-such as headaches and dizziness. These symptoms impose a significant burden, yet their underlying mechanisms remain unclear.

Predictive processing theories suggest that persistent symptoms may result from learned perceptual errors, particularly in individuals with high negative affectivity. This framework may help explain ongoing persistent post-concussive symptoms (PPCS) in the absence of identifiable pathology, which have been linked to various psychological factors.

Mental imagery (MI) is thought to engage similar predictive processes. There is evidence that MI of symptom-triggering movements may exacerbate symptoms in individuals with chronic somatic conditions. However, this phenomenon has not been studied in PPCS patients. Investigating symptom provocation through MI may yield novel insights into the neuropsychological mechanisms sustaining PPCS and potentially contribute to the development of therapeutic tools for this population.

Objectives:

1. Documenting the exacerbation of headache and dizziness following provocative mental imagery (imagery of movements or scenarios that elicit these symptoms in real life) in patients with PPCS. 2. Comparing changes in headache and dizziness after provocative MI versus neutral MI (imagery of movements or scenarios that do not elicit these symptoms in real life). 3. Comparing patients who experience symptom exacerbation following mental imagery to those who do not. 4. Describing associations between symptom exacerbation and negative affectivity, anxiety, depression, catastrophizing, and lower daily functioning.

Methods: A single-group, open-label experimental provocation study is being conducted in adult patients with persistent post-concussive symptoms following mild traumatic brain injury. Each participant undergoes all imagery conditions, with the order of provocative and neutral mental imagery stimuli randomized within participants. Participants are recruited by convenience sampling from the computerized patient database of Reuth Rehabilitation Hospital according to the inclusion and exclusion criteria.

After signing an informed consent form, participants will be invited to attend 2 to 3 sessions, each lasting 1 to 2 hours. During these sessions, a licensed physiotherapist will conduct a comprehensive clinical assessment, including: Completion of self-report questionnaires; A vestibular examination; Anamnestic interview and clinical assessment of individual movement- and scenario-related triggers for dizziness and headaches; Symptom provocation testing using mental imagery of the identified triggers.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Current patients of Reut Rehabilitation Hospital or individuals who were discharged from the hospital within the past 12 months.

Diagnosis of mild Traumatic Brain Injury, concussion, blast injury, or cervical whiplash injury.

More than 3 months since the event.

Presence of headaches and/or dizziness that began after the injury and have persisted continuously or intermittently.

Disqualifiers

Significant cognitive impairment preventing informed consent (Mini-Mental State Examination score <20 or Montreal Cognitive Assessment score <20, as per IRB requirements).

Diagnosed central neurological conditions such as multiple sclerosis, Parkinson's disease, stroke, or brain tumor.

Presence of known pyramidal or extrapyramidal neurological signs.

Significant language impairment interfering with communication.

Trial design

Design model

Single group

Treatments tested in this trial

  • Provocation Test for Symptoms Using Mental Imagery

    Other intervention

    • The mental imagery task will be guided by the examiner through continuous verbal instruction (the examiner will provide ongoing instructions throughout the entire task, not just at the beginning). During the instruction, the examiner will direct the participant's attention to visual, auditory, and proprioceptive aspects of the imagined movement or scenario. Example: "Close your eyes, and without moving your head or body at all, try to imagine that you are moving your head from side to side quickly and easily, while noticing the sensation of motion, seeing the rotation through your eyes, and feeling the acceleration of your head as it moves from side to side..."

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Mental Imagery Provocation TestingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Headache intensity Change

Measured on a 100mm Visual Analog Scale from 0 ("no Pain") to 100 ("most severe Pain")

Time frame
Immediately before and after the intervention at assessment session 2
2

Dizziness intensity change

Measured on a 100mm Visual Analog Scale from 0 ("no dizziness") to 100 ("most severe dizziness")

Time frame
Immediately before and after the intervention at assessment session 2

Secondary outcomes

1

Headache Impact on Daily life

Headache Impact Test-6 (HIT-6): A brief assessment tool used to measure the impact of headaches on daily life. The questionnaire includes six questions addressing the frequency of functional impairment, pain intensity, and quality of life related to headaches

Time frame
Within 1-2 weeks before the intervention
2

Post-Concussion Symptoms

Rivermead Post-Concussion Symptoms Questionnaire (RPQ): A questionnaire assessing the severity of post-concussion symptoms. It includes 16 items where participants rate their symptoms compared to their pre-injury state on a Likert scale from 0 ("not experienced at all") to 4 ("severe problem").

Time frame
Within 1-2 weeks before the intervention
3

Perceived disability due to dizziness

Dizziness Handicap Inventory (DHI): A questionnaire assessing the level of disability caused by dizziness. It consists of 25 items and provides a score in percentages, where 100% indicates a high level of perceived self-disability.

Time frame
Within 1-2 weeks before the intervention
4

Pain Catastrophizing

Pain Catastrophizing Scale - A questionnaire assessing catastrophic thoughts related to pain, consisting of 13 items rated on a scale from 0 ("Never") to 4 ("Very much"). A high score indicates a tendency toward catastrophizing-exaggerated negative thoughts, helplessness, and magnification in response to pain.

Time frame
Within 1-2 weeks before the intervention

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.